The cytotoxic and antiproliferative effect of Polygala saponin XLIV on the human colorectal carcinoma cell line
| dc.contributor.author | Becer, Eda | |
| dc.contributor.author | Hanoglu, Azmi | |
| dc.contributor.author | Unlu, Ayse | |
| dc.contributor.author | Aydin, Zuebeyde Ugurlu | |
| dc.contributor.author | Donmez, Ali A. | |
| dc.contributor.author | Jurt, Simon | |
| dc.contributor.author | Calis, Ihsan | |
| dc.date.accessioned | 2026-02-06T18:26:30Z | |
| dc.date.issued | 2025 | |
| dc.department | Doğu Akdeniz Üniversitesi | |
| dc.description.abstract | Objectives Saponins are secondary metabolites naturally found in plants with diverse pharmacological properties such as anticancer. This research aimed to explore the anti-cancer properties of Polygalasaponin XLIV (PS-XLIV) in a human colorectal carcinoma cell line derived from Polygala vulgaris roots.Methods HCT166 cells were treated with different PS-XLIV concentrations and incubated for 24 and 48 h. We used immunocytochemistry to investigate PS-XLIV's anti-cancer properties, employing antibodies targeting WNT3A, WNT11, STAT3, beta-catenin, and Ki-67. The IC50 value of PS-XLIV was 80 mu g/mL in HCT116 cells. WNT11, STAT3, beta-catenin, and Ki-67. Immunoreactivities significantly decreased in PS-XLIV-treated HCT116 cells than in control group cells.Results After PS-XLIV treatment, the epithelial morphology of cells was protected; however, the number of cells was less than that of the control group cells. While WNT3A immunoreactivity was similar in both groups, WNT11 and beta-catenin immunoreactivities were decreased after PS-XLIV application. In addition, the PS-XLIV treated group exhibited significantly weaker Ki-67 immunoreactivity, STAT3 immunoreactivty was moderated after PS-XLIV application.Conclusions For the first time, the anticancer effects of PS-XLIV isolated from P. vulgaris on HCT116 cells were shown. The anticancer effect may involve PS-XLIV reducing WNT11, beta-catenin, STAT3, and Ki-67 activation pathways in HCT116 cells. | |
| dc.description.sponsorship | TUEBITAK [118 Z 708] | |
| dc.description.sponsorship | We are grateful to TUB & Idot;TAK (Project No. 118 Z 708) for the financial support and Julia Brunner (Regensburg University, Germany) for her kind help in the literature search. | |
| dc.identifier.doi | 10.1515/tjb-2024-0215 | |
| dc.identifier.endpage | 212 | |
| dc.identifier.issn | 0250-4685 | |
| dc.identifier.issn | 1303-829X | |
| dc.identifier.issue | 2 | |
| dc.identifier.orcid | 0000-0001-5489-3420 | |
| dc.identifier.orcid | 0000-0001-6695-6177 | |
| dc.identifier.orcid | 0000-0002-7586-9080 | |
| dc.identifier.orcid | 0000-0002-7415-9618 | |
| dc.identifier.orcid | 0000-0002-2378-128X | |
| dc.identifier.orcid | 0000-0002-1113-3074 | |
| dc.identifier.orcid | 0000-0002-6016-8505 | |
| dc.identifier.scopus | 2-s2.0-105004053785 | |
| dc.identifier.scopusquality | Q3 | |
| dc.identifier.startpage | 205 | |
| dc.identifier.trdizinid | 1359390 | |
| dc.identifier.uri | https://doi.org/10.1515/tjb-2024-0215 | |
| dc.identifier.uri | https://search.trdizin.gov.tr/tr/yayin/detay/1359390 | |
| dc.identifier.uri | https://hdl.handle.net/11129/10516 | |
| dc.identifier.volume | 50 | |
| dc.identifier.wos | WOS:001390043100001 | |
| dc.identifier.wosquality | Q4 | |
| dc.indekslendigikaynak | Web of Science | |
| dc.indekslendigikaynak | Scopus | |
| dc.indekslendigikaynak | TR-Dizin | |
| dc.language.iso | en | |
| dc.publisher | Walter De Gruyter Gmbh | |
| dc.relation.ispartof | Turkish Journal of Biochemistry-Turk Biyokimya Dergisi | |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.snmz | KA_WoS_20260204 | |
| dc.subject | cancer | |
| dc.subject | colon | |
| dc.subject | Polygala vulgaris | |
| dc.subject | saponin | |
| dc.title | The cytotoxic and antiproliferative effect of Polygala saponin XLIV on the human colorectal carcinoma cell line | |
| dc.type | Article |










